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Human Factors Design Process for Medical Devices
standard by Association for the Advancement of Medical Instrumentation, 10/01/2001
Description
The purpose of this process-oriented standard is to provide ergonomic information and human factors engineering guidance so that optimum user and patient safety, system safety and performance, and operator effectiveness will be reflected in medical device design. This document describes a recommended human factors engineering process for use in fulfilling user interface design requirements in the development of medical devices and systems, including hardware, software, and documentation.
Product Details
- Published:
- 10/01/2001
- ANSI:
- ANSI Approved
- Number of Pages:
- 48
- File Size:
- 1 file , 480 KB
- Note:
- This product is unavailable in Russia, Ukraine, Belarus
